Canonical Allele Identifier: CA1988808631

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951927G= , CM000673.2:g.86951927G= GRCh38
NC_000011.9:g.86662969G= , CM000673.1:g.86662969G= GRCh37
NC_000011.8:g.86340617G= NCBI36
NG_011752.1:g.8465C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.829C= (FZD4) MANE Select ENSP00000434034.1:p.Arg277=
ENST00000531380.1:c.829C= (FZD4) ENSP00000434034.1:p.Arg277=
ENST00000532234.5:c.*920G= (PRSS23) ENSP00000436676.1:n.*920G=
ENST00000533902.2:c.*642G= (PRSS23) ENSP00000437268.1:n.*642G=
NM_012193.3:c.829C= (FZD4) NP_036325.2:p.Arg277=
NR_120591.1:n.1592G= (PRSS23)
NR_120592.1:n.1341G= (PRSS23)
NR_120591.2:n.1290G= (PRSS23)
NR_120592.2:n.1039G= (PRSS23)
NM_012193.4:c.829C= (FZD4) MANE Select NP_036325.2:p.Arg277=
NR_120591.3:n.1290G= (PRSS23)